Canonical Allele Identifier: PA2827326230
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 189058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Gly865Asp
CA274329
NM_001330578.2:c.2594G>A